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Connective tissue growth factor-mediated upregulation of neuromedin U expression in trabecular meshwork cells and its role in homeostasis of aqueous humor outflow.

Publication ,  Journal Article
Iyer, P; Maddala, R; Pattabiraman, PP; Rao, PV
Published in: Invest Ophthalmol Vis Sci
July 26, 2012

PURPOSE: Connective tissue growth factor (CTGF) is a matricellular protein presumed to be involved in the pathobiology of various fibrotic diseases, including glaucoma. We investigated the effects of Rho GTPase-dependent actin cytoskeletal integrity on CTGF expression and CTGF-induced changes in gene expression profile in human trabecular meshwork (HTM) cells. METHODS: CTGF levels were quantified by immunoblotting and ELISA. CTGF-induced changes in gene expression, actin cytoskeleton, myosin light chain (MLC) phosphorylation, and extracellular matrix (ECM) proteins were evaluated in trabecular meshwork (TM) cells by cDNA microarray, q-PCR, fluorescence microscopy, and immunoblot analyses. The effects of neuromedin U (NMU) on aqueous humor (AH) outflow were determined in enucleated porcine eyes. RESULTS: Expression of a constitutively active form of RhoA (RhoAV14), activation of Rho GTPase by bacterial toxin, or inhibition of Rho kinase by Y-27632 in HTM cells led to significant but contrasting changes in CTGF protein levels that were detectable in cell lysates and cell culture medium. Stimulation of HTM cells with CTGF for 24 hours induced actin stress fiber formation, and increased MLC phosphorylation, fibronectin, and laminin levels, and NMU expression. NMU independently induced actin stress fibers and MLC phosphorylation in TM cells, and decreased AH outflow facility in perfused porcine eyes. CONCLUSIONS: These data revealed that CTGF influences ECM synthesis, actin cytoskeletal dynamics, and contractile properties in TM cells, and that the expression of CTGF is regulated closely by Rho GTPase. Moreover, NMU, whose expression is induced in response to CTGF, partially mimics the effects of CTGF on actomyosin organization in TM cells, and decreases AH outflow facility, revealing a potentially important role for this neuropeptide in the homeostasis of AH drainage.

Duke Scholars

Published In

Invest Ophthalmol Vis Sci

DOI

EISSN

1552-5783

Publication Date

July 26, 2012

Volume

53

Issue

8

Start / End Page

4952 / 4962

Location

United States

Related Subject Headings

  • rhoA GTP-Binding Protein
  • Up-Regulation
  • Trabecular Meshwork
  • Swine
  • Phosphorylation
  • Ophthalmology & Optometry
  • Neuropeptides
  • Homeostasis
  • Gene Expression Profiling
  • Extracellular Matrix Proteins
 

Citation

APA
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ICMJE
MLA
NLM
Iyer, P., Maddala, R., Pattabiraman, P. P., & Rao, P. V. (2012). Connective tissue growth factor-mediated upregulation of neuromedin U expression in trabecular meshwork cells and its role in homeostasis of aqueous humor outflow. Invest Ophthalmol Vis Sci, 53(8), 4952–4962. https://doi.org/10.1167/iovs.12-9681
Iyer, Padma, Rupalatha Maddala, Padmanabhan P. Pattabiraman, and Ponugoti Vasantha Rao. “Connective tissue growth factor-mediated upregulation of neuromedin U expression in trabecular meshwork cells and its role in homeostasis of aqueous humor outflow.Invest Ophthalmol Vis Sci 53, no. 8 (July 26, 2012): 4952–62. https://doi.org/10.1167/iovs.12-9681.
Iyer, Padma, et al. “Connective tissue growth factor-mediated upregulation of neuromedin U expression in trabecular meshwork cells and its role in homeostasis of aqueous humor outflow.Invest Ophthalmol Vis Sci, vol. 53, no. 8, July 2012, pp. 4952–62. Pubmed, doi:10.1167/iovs.12-9681.

Published In

Invest Ophthalmol Vis Sci

DOI

EISSN

1552-5783

Publication Date

July 26, 2012

Volume

53

Issue

8

Start / End Page

4952 / 4962

Location

United States

Related Subject Headings

  • rhoA GTP-Binding Protein
  • Up-Regulation
  • Trabecular Meshwork
  • Swine
  • Phosphorylation
  • Ophthalmology & Optometry
  • Neuropeptides
  • Homeostasis
  • Gene Expression Profiling
  • Extracellular Matrix Proteins